GE Parallel Design Inc
⚠️ Moderate Risk
FEI: 3003309342 • Phoenix, AZ • UNITED STATES
FEI Number
3003309342
Location
Phoenix, AZ
Country
UNITED STATESAddress
4313 E Cotton Center Blvd Ste 100, , Phoenix, AZ, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/19/2023 | 90ITXTRANSDUCER, ULTRASONIC, DIAGNOSTIC | Division of Northern Border Imports (DNBI) | |
| 2/5/2015 | 90IYNSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC | Chicago District Office (CHI-DO) | |
| 3/4/2014 | 90IYNSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC | 16DIRECTIONS | Los Angeles District Office (LOS-DO) |
| 10/21/2013 | 90ITXTRANSDUCER, ULTRASONIC, DIAGNOSTIC | 341REGISTERED | Detroit District Office (DET-DO) |
| 1/27/2005 | 90ITXTRANSDUCER, ULTRASONIC, DIAGNOSTIC | 341REGISTERED | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is GE Parallel Design Inc's FDA import refusal history?
GE Parallel Design Inc (FEI: 3003309342) has 5 FDA import refusal record(s) in our database, spanning from 1/27/2005 to 1/19/2023.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. GE Parallel Design Inc's FEI number is 3003309342.
What types of violations has GE Parallel Design Inc received?
GE Parallel Design Inc has been cited for 7 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about GE Parallel Design Inc come from?
All FDA import refusal data for GE Parallel Design Inc is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.